a)
It is not possible to identify the product from the serial number and
production date on the bed.
b)
The product has been used in a manner inconsistent with the manner
described in the instruction manual. The product has been used for other
purposes or in conditions other than the intended ones.
c)
There has been an interference with the product, including repair of the
product by an entity other than the manufacturer or authorized service
of Reha-Bed.
d)
The product has been mechanically damaged (e. g. fall, hit, breaking the
railings by leaning or sitting on the product, etc.).
e)
The product was damaged as a result of external factors
–
e. g. through
contamination, flooding of actuators or the control box, use of the bed
in inadequate conditions and if the product was damaged due to the
user’s fault (e. g. during the use of a damaged product or inappropriate
equipment, overloading the bed, etc.).
f)
The product was used despite the defect.
g)
The product was damaged during transportation.
h)
The product (delivered for repair) is incomplete.
i)
Non-compliance with notes and warnings presented in the instruction
manual.
Consideration of the complaint refers only to products placed on the market
by the manufacturer
–
Reha-Bed Sp. z o.o.
Summary of Contents for Leo Med
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